Mendine Pharmaceuticals Pvt. Ltd., a WHO-GMP and ISO 9001:2015 certified pharmaceutical company, is hiring Regulatory Affairs Interns for its Quality Assurance Department in Kolkata. This is an excellent opportunity for M.Pharm (Regulatory Affairs) freshers to gain hands-on experience in regulatory compliance, dossier submissions, and documentation under industry experts.
✅ Key Responsibilities:
- Assist in preparing test licenses, regulatory dossiers, and submissions.
- Handle endorsement documents, SOP drafting, and ONDLS portal management.
- Support regulatory notifications, compliance updates, and documentation.
- Coordinate with QA & RA teams for regulatory filings and approvals.
- Ensure adherence to WHO-GMP, CDSCO, and other regulatory guidelines.
🏢 About Mendine Pharmaceuticals
Mendine Pharmaceuticals is a reputed pharmaceutical company with a strong commitment to quality, compliance, and patient safety. With decades of expertise, the company operates under WHO-GMP and ISO-certified facilities, ensuring global healthcare standards.
🌟 Why Join Mendine Pharmaceuticals?
✔ WHO-GMP Certified Environment – Work in a globally compliant setup.
✔ Real-World Regulatory Exposure – Learn from industry professionals.
✔ Career Growth Opportunities – Enhance your skills in pharmaceutical regulations.
✔ Dynamic Work Culture – Collaborative and learning-focused environment.
🎓 Who Can Apply?
📜 Required Qualifications:
- M.Pharm in Regulatory Affairs (2023/2024 pass-outs preferred).
- Strong interest in pharmaceutical regulations and compliance.
💡 Preferred Skills:
- Basic knowledge of MS Word & Excel.
- Understanding of regulatory guidelines (CDSCO, WHO-GMP, ICH).
- Attention to detail and strong documentation skills.
📩 How to Apply?
Interested candidates should email their updated CV to:
📧 Email: piyali.basu@mendine.com
